Cas 110465-39-9,1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one

110465-39-9

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Basic information

Product Name: 1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one
Synonyms:
CAS NO:110465-39-9
Molecular Formula:
Molecular Weight: 445.369
EINECS: N/A
Product Categories: N/A
Mol File: 110465-39-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(110465-39-9)
EPA Substance Registry System: 1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(110465-39-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 110465-39-9(Hazardous Substances Data)

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1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one
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1,3-Bis-(4-chloro-phenyl)-5,7,7-trimethyl-2-thioxo-1,2,3,7-tetrahydro-pyrano[2,3-d]pyrimidin-4-one
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110465-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110465-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,4,6 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110465-39:
(8*1)+(7*1)+(6*0)+(5*4)+(4*6)+(3*5)+(2*3)+(1*9)=89
89 % 10 = 9
So 110465-39-9 is a valid CAS Registry Number.

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110465-39-9Relevant articles and documents

A NOVEL ONE STEP SYNTHESIS OF PYRANO(2,3-d) PYRIMIDINES

Ahluwalia, V. K.,Sharma, H. R.,Tyagi, Renu

, p. 4045 - 4048 (1986)

A novel one step synthesis of pyrano(2,3-d) pyrimidines is described.It utilises the reaction different barbituric acid with ketones.

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